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微小RNA-20b下调着色性干皮病变异型肿瘤细胞中的聚合酶κ和θ。

miR-20b downregulates polymerases κ and θ in XP-V tumor cells.

作者信息

Guo Jia, Jiang Zheng, Li Xiangru, Wang X I, Xiao Yan

机构信息

Department of Endodontics, Oral Medical Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, P.R. China.

Department of Endodontics, Xiamen Stomatological Hospital, Xiamen, Fujian 361004, P.R. China.

出版信息

Oncol Lett. 2016 Jun;11(6):3790-3794. doi: 10.3892/ol.2016.4447. Epub 2016 Apr 18.

Abstract

XP-V is a subtype of Xeroderma pigmentosum diseases with typical pigmentation and cancers in sun-exposed regions. The present study investigated the role of microRNA-20b (miR-20b) in the imbalance of polymerase expression levels in XP-V tumor cells. Following software prediction results, certain miRNAs were chosen as candidate regulators for the observed imbalance in polymerases in XP-V tumor cells. Reverse transcription-quantitative polymerase chain reaction and western blot were used to test candidate miRNAs for their ability to reduce the expression of these polymerases. A luciferase reporter assay was used to further verify the western blot results. Polymerases κ and θ were expressed at lower levels in XP-V tumor cells compared to normal control cells. A positive correlation was demonstrated between miR-20b and polymerases κ and θ. It was also demonstrated that a proportion of miRNAs had no effect on polymerases κ and θ, despite the software predicting that these miRNAs would target these two polymerases. Therefore, miR-20b may be responsible for the low expression levels of polymerase κ and θ in XP-V tumor cells, which accelerated mismatch in DNA replication repairing.

摘要

着色性干皮病变异型(XP-V)是着色性干皮病的一种亚型,在阳光暴露部位有典型的色素沉着和癌症。本研究调查了微小RNA-20b(miR-20b)在XP-V肿瘤细胞中聚合酶表达水平失衡中的作用。根据软件预测结果,选择了某些微小RNA作为XP-V肿瘤细胞中观察到的聚合酶失衡的候选调节因子。采用逆转录定量聚合酶链反应和蛋白质印迹法检测候选微小RNA降低这些聚合酶表达的能力。使用荧光素酶报告基因检测进一步验证蛋白质印迹结果。与正常对照细胞相比,XP-V肿瘤细胞中聚合酶κ和θ的表达水平较低。miR-20b与聚合酶κ和θ之间呈正相关。还证明,尽管软件预测这些微小RNA会靶向这两种聚合酶,但一部分微小RNA对聚合酶κ和θ没有影响。因此,miR-20b可能是XP-V肿瘤细胞中聚合酶κ和θ低表达水平的原因,这加速了DNA复制修复中的错配。

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Molecular genetics of Xeroderma pigmentosum variant.着色性干皮病变异型的分子遗传学
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